42 C.F.R. § 11.6

Current through November 30, 2024
Section 11.6 - What are the requirements for the submission of truthful information?

The clinical trial information submitted by a responsible party under this part shall not be false or misleading in any particular. A responsible party who submits false and/or misleading information is subject to civil monetary penalties and/or other civil or criminal remedies available under U.S. law.

42 C.F.R. §11.6

81 FR 65138 , 1/18/2017